Works by Sher, Roger B.
Results: 13
Embryonic Exposure to the Environmental Neurotoxin BMAA Negatively Impacts Early Neuronal Development and Progression of Neurodegeneration in the Sod1-G93R Zebrafish Model of Amyotrophic Lateral Sclerosis.
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- Toxicological Sciences, 2017, v. 157, n. 1, p. 129, doi. 10.1093/toxsci/kfx020
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- Article
NEMF mutations in mice illustrate how Importin-β specific nuclear transport defects recapitulate neurodegenerative disease hallmarks.
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- PLoS Genetics, 2024, v. 20, n. 9, p. 1, doi. 10.1371/journal.pgen.1011411
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- Article
Muscle choline kinase beta defect causes mitochondrial dysfunction and increased mitophagy.
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- Human Molecular Genetics, 2011, v. 20, n. 19, p. 3841, doi. 10.1093/hmg/ddr305
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- Article
Mdm muscular dystrophy: interactions with calpain 3 and a novel functional role for titin's N2A domain.
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- Human Molecular Genetics, 2005, v. 14, n. 19, p. 2801, doi. 10.1093/hmg/ddi313
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- Article
Genetic Background Effects on Disease Onset and Lifespan of the Mutant Dynactin p150<sup>Glued</sup> Mouse Model of Motor Neuron Disease.
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- PLoS ONE, 2015, v. 10, n. 3, p. 1, doi. 10.1371/journal.pone.0117848
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- Article
A major QTL on mouse chromosome 17 resulting in lifespan variability in SOD1-G93A transgenic mouse models of amyotrophic lateral sclerosis.
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- Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration, 2014, v. 15, n. 7/8, p. 588, doi. 10.3109/21678421.2014.932381
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- Article
The SATB1‐MIR22‐GBA axis mediates glucocerebroside accumulation inducing a cellular senescence‐like phenotype in dopaminergic neurons.
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- Aging Cell, 2024, v. 23, n. 4, p. 1, doi. 10.1111/acel.14077
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- Article
Identification of quantitative trait loci for survival in the mutant dynactin p150Glued mouse model of motor neuron disease.
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- PLoS ONE, 2022, v. 17, n. 9, p. 1, doi. 10.1371/journal.pone.0274615
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- Article
Functional rescue in a mouse model of congenital muscular dystrophy with megaconial myopathy.
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- Human Molecular Genetics, 2019, v. 28, n. 16, p. 2635, doi. 10.1093/hmg/ddz068
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- Article
Author Correction: NEMF mutations that impair ribosome-associated quality control are associated with neuromuscular disease.
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- 2020
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- Correction Notice
NEMF mutations that impair ribosome-associated quality control are associated with neuromuscular disease.
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- Nature Communications, 2020, v. 11, n. 1, p. N.PAG, doi. 10.1038/s41467-020-18327-6
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- Article
NEMF mutations that impair ribosome-associated quality control are associated with neuromuscular disease.
- Published in:
- Nature Communications, 2020, v. 11, n. 1, p. N.PAG, doi. 10.1038/s41467-020-18327-6
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- Article
Rhabdomyosarcomas in Aging A/J Mice.
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- PLoS ONE, 2011, v. 6, n. 8, p. 1, doi. 10.1371/journal.pone.0023498
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- Article